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Improved assay for genotyping haemophilia A carriers with intron 22 dinucleotide repeat marker

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Title Improved assay for genotyping haemophilia A carriers with
intron 22 dinucleotide repeat marker
 
Creator Saha, A
Mukherjee, S
Ray, Kunal
 
Subject Molecular & Human Genetics
 
Description Haemophilia A, the most common bleeding disorder
caused by defects in the Factor VIII gene (FVIII),
affects one in 5000 males worldwide. Due to the
inherent instability of the gene, caused by the
presence of multiple copies of the same genomic
regions, de novo mutation accounts for 40–50% of
the gene defects. In addition, heterogeneous mutations
have been detected covering its entire length
 
Date 2006
 
Type Article
PeerReviewed
 
Format application/pdf
 
Identifier http://www.eprints.iicb.res.in/464/1/HAEMOPHILIA%2C12(_2)%2C_200%2D201[126].pdf
Saha, A and Mukherjee, S and Ray, Kunal (2006) Improved assay for genotyping haemophilia A carriers with intron 22 dinucleotide repeat marker. Haemophilia, 12 (2). pp. 200-201.
 
Relation htpp://dx.doi.org/10.1111/j.1365-2516.2006.01205.x
http://www.eprints.iicb.res.in/464/